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hemorrhoidal - 56062-678-64 - (Mineral oil, petrolatum, phenylephrine hcl)

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Drug Information of hemorrhoidal

Product NDC: 56062-678
Proprietary Name: hemorrhoidal
Non Proprietary Name: Mineral oil, petrolatum, phenylephrine hcl
Active Ingredient(s): 140; 719; 2.5    mg/100g; mg/100g; mg/100g & nbsp;   Mineral oil, petrolatum, phenylephrine hcl
Administration Route(s): RECTAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of hemorrhoidal

Product NDC: 56062-678
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121119

Package Information of hemorrhoidal

Package NDC: 56062-678-64
Package Description: 1 TUBE in 1 CARTON (56062-678-64) > 28 g in 1 TUBE

NDC Information of hemorrhoidal

NDC Code 56062-678-64
Proprietary Name hemorrhoidal
Package Description 1 TUBE in 1 CARTON (56062-678-64) > 28 g in 1 TUBE
Product NDC 56062-678
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Mineral oil, petrolatum, phenylephrine hcl
Dosage Form Name OINTMENT
Route Name RECTAL
Start Marketing Date 20121119
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 140; 719; 2.5
Strength Unit mg/100g; mg/100g; mg/100g
Pharmaceutical Classes

Complete Information of hemorrhoidal


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